alexa Hemolytic Anemia Online Journals | OMICS Group |Hematology-Thromboembolic-Diseases

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Hemolytic Anemia

Autoimmune hemolytic anemia (AIHA) is caused by hemolysis induced by the reaction of autoantibodies with red blood cells (RBCs). Events that lead to AIHA include extravascular hemolysis caused by phagocytosis of erythrocyte-bound IgG in the spleen (hemolytic mechanism), activation of polyclonal B cells, reactions induced by molecular mimicry of exogenous antigens, breakdown of immune tolerance, and abnormal cytokine expression (autoimmune mechanism). Evans syndrome is diagnosed by the simultaneous presence of AIHA, which is detected using a direct antiglobulin test (DAT), and immune (idiopathic) thrombocytopenic purpura (ITP) in the absence of an underlying etiology. This syndrome is characterized by hemolytic anemia, thrombocytopenia, and the production of either antibodies, or complement, or both that attack RBCs and platelets. Online Journals are scholarly and peer reviewed journals. The journals provide forum and motivates scientists, researchers, academics, engineers, and practitioners in all aspects to share their professional and academic knowledge in the fields computing, engineering, humanities, economics, social sciences, management, medical science, and related disciplines. Online Journals also aims to reach a large number of readers worldwide with original and current research work completed on the vital issues of the above important disciplines. The journals permit all readers to read, view, download and print the full-text of all published articles without any subscription or restrictions.
 
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